ENST00000682617.1:c.2104C>G
|
ENSP00000507912.1:p.Leu702Val
|
|
ENST00000683962.1:c.*1660C>G
|
ENSP00000506854.1:n.*1660C>G
|
|
ENST00000311895.8:c.1966C>G
MANE Select
|
ENSP00000310520.7:p.Leu656Val
|
|
ENST00000311895.7:c.1966C>G
|
ENSP00000310520.7:p.Leu656Val
|
|
ENST00000389138.7:n.1243C>G
|
|
|
ENST00000462862.1:c.279C>G
|
ENSP00000461322.1:n.279C>G
|
|
NM_005236.2:c.1966C>G , LRG_463t1:c.1966C>G
|
NP_005227.1:p.Leu656Val
|
|
XM_011522424.1:c.2104C>G
|
XP_011520726.1:p.Leu702Val
|
|
XM_011522425.1:c.1423C>G
|
XP_011520727.1:p.Leu475Val
|
|
XM_011522426.1:c.1177C>G
|
XP_011520728.1:p.Leu393Val
|
|
XM_011522427.1:c.616C>G
|
XP_011520729.1:p.Leu206Val
|
|
XR_932805.1:n.2125C>G
|
|
|
XM_011522424.3:c.2104C>G
|
XP_011520726.1:p.Leu702Val
|
|
XM_017023043.2:c.1177C>G
|
XP_016878532.1:p.Leu393Val
|
|
NM_005236.3:c.1966C>G
MANE Select
|
NP_005227.1:p.Leu656Val
|
|